ライフサイエンスコーパス: voltage

1 site characteristics appeared with high bias voltage.

2 fferent modulation effects by an applied tip voltage.

3 can be controlled by simply tuning the spray voltage.

4 ses can be controlled by varying the applied voltage.

5 the mechanisms changes with the induced bias voltage.

6 -/multiple epoxides is achieved at different voltages.

7 m of the threshold voltage shift to negative voltages.

8 on insertion to produce shape changes at low voltages.

9 MCs), as they lose oxygen at lower operating voltages.

10 n spectra of the modulator at different gate voltages.

11 ect on the following ozonation, but a higher-voltage (0.6-1.2 V) LEEFT significantly enhances the ozo

12 This results in a much smaller Dirac voltage (- 1 V) and hysteresis (0.9 V) when compared to

13 The maximum voltages (160, 183, 260, 292, and 342 mV) of the constru

14 lectrochemical actuators that operate at low voltages (200 microvolts), low power (10 nanowatts) and

15 electric constant (~100) and large breakdown voltage (~5.7 GV m(-1)).

16 trogram fractionation even in the absence of voltage abnormalities.

17 the salty receptor, is co-expressed with the voltage-activated ATP release channel CALHM1/3 in a subs

18 showing that MDIMP preferentially blocks low-voltage-activated channels.

19 .1 and other Ca(V)2 channels, including high voltage-activated currents that are larger in external B

20 The M-current is a low voltage-activated potassium current generated by neurona

21 sent electrophysiological evidence that TPC3 voltage activation depends only on voltage sensing domai

22 sion events that are associated with EEG low voltage activity events, which correlate with transient

23 re activated by voltage and Ca(2+), and that voltage and Ca(2+) activations interact, less is known a

24 ndicators like GCaMP to provide simultaneous voltage and Ca(2+) imaging.

25 t is known that BK channels are activated by voltage and Ca(2+), and that voltage and Ca(2+) activati

26 citation via bi-directional coupling between voltage and Ca2+, forming a delayed feedback loop.

27 ams; microwave ablation caused reductions in voltage and changes in electrogram morphology with loss

28 cting several devices linearly scales up the voltage and current to power electronics.

29 oton-counting detector CT, depending on tube voltage and energy threshold combination.

30 Using voltage and extracellular glutamate transient recording

31 We probe how these motions depend on voltage and frequency of oscillating field applied in an

32 We attribute the low voltage and high rate capability of disordered rock salt

33 ally and independently activated by membrane voltage and intracellular Ca(2+).

34 he mean and variances of the non-thresholded voltage and its rate of change in neuronal structures su

35 Detailed magnetic, current/voltage and low-energy electron energy loss spectroscopy

36 Mean delivered peak voltage and peak current were 2154+/-59 V and 33.9+/-1.6

37 rift time IMS without employing higher drift voltages and bulky power supplies.

38 mited by the inferior performance under high voltages and challenging temperatures.

39 endomyocardial biopsy showed low endocardial voltages and fibro-fatty replacement in areas of late ga

40 ons are highly sensitive to the transmission voltages and the analysis time scale.

41 s to activate at significantly more negative voltages and with slower deactivation kinetics than the

42 specific inhibitor of the large-conductance, voltage- and Ca(2+)-dependent BK-type K(+) channel.

43 ctivation of these paralogs differs from the voltage- and calcium-gated channel CALHM1.

44 nto pseudovoltage-clamp mode (for concurrent voltage application and current recording).

45 the generated high-voltage for practical low-voltage applications is still under investigation.

46 aters A and B (or B and C) and adjusting the voltage applied on microheater A (or C).

47 body, showing an "anti-aging" effect in high-voltage battery cycling and successfully stopping the es

48 ), solvent type, process parameters (applied voltage between the needle tip and the collector surface

49 show that the application of a minimal gate voltage bias can induce stress in the channel layer as h

50 y converts chemical energy into a persistent voltage bias that can power electronic circuits.

51 e physiological parameters, such as membrane voltage, calcium, pH, and redox potential.

52 neuECG is voltage calibrated and does not require invasive procedu

53 uctive lithium (Li) metal anode and the high-voltage cathode for long-life, high-energy-density recha

54 le above 4 V, which prevents the use of high-voltage cathodes that promise higher energy densities.

55 tion and alterations in the maximal rates of voltage change during spike depolarization and repolariz

56 how S4 moves through a hydrophobic plug upon voltage changes, the possible helix transition from alph

57 then a phase with strongly nonlinear current-voltage characteristics, suggestive of a pinned Wigner s

58 cell anion channel activity, recorded under voltage clamp, follows KfSLAC1 and KfALMT12 transcript a

59 Using whole-cell voltage clamp, we discovered that enhancing S-palmitoyla

60 Each methylnicotine was investigated using voltage-clamp and radioligand binding techniques.

61 Dual voltage-clamp experiments substantiate low resistance el

62 tate KCNQ1 conductance is demonstrated using voltage-clamp fluorometry.

63 In voltage-clamp oocyte studies using the ubiquitous amanta

64 ences between rod flash responses and recent voltage-clamp recordings of cone flash responses, using

65 (+)-K(+) pump current, I(p), was measured in voltage-clamped myocytes from noninfarct myocardium.

66 In voltage-clamped, intact Casq2-/- cardiomyocytes pretreat

67 ICE 4: Monopolar hemostatic forceps with low-voltage coagulation can be an effective alternative to o

68 integrated logic circuits with low switching voltages compatible with standard CMOS electronics.

69 me this barrier by developing a new class of voltage-controllable electrochemical actuators that oper

70 croreactor has unique features that allow i) voltage-controlled acceleration of electrochemical react

71 findings open up this class of materials for voltage-controlled functionality.

72 We report herein a voltage-controlled interfacial microreactor that enables

73 ly, OLC-FCDI), in this work, we analyzed the voltage-current (V-I) characteristics of several FCDI un

74 and robust systems for EME operated at high voltage/current and for EME performed in narrow channels

75 alter the shape of the instantaneous current-voltage curve, and substituting one or two residues in t

76 The relation between open-circuit voltage, dark current, and noise current is demonstrated

77 hemical performance, with a very low average voltage decay of 0.8 mV per cycle as well as a capacity

78 It however suffers from a voltage decay upon cycling, urging for an in-depth under

79 ent-tailored LLOs exhibit noticeably reduced voltage decay, enhanced rate performance, improved cycle

80 rtion would induce serious capacity loss and voltage decay, further hindering its practical applicati

81 The antibodies shift the voltage dependence of activation and slow the deactivati

82 Here we reverse the voltage dependence of HCN channels by mutating only two

83 e changes accompanied negative shifts in the voltage dependence of I(Na) inactivation (within 10 min)

84 at S4 induces a large depolarizing shift in voltage dependence of K(v)7.2 channels and L268F at the

85 ch clamp experiments, we discovered a robust voltage dependence of the thromboxane receptor (TP recep

86 ggests a closed pore consistent with extreme voltage dependence.

87 activated with iloprost showed no detectable voltage dependence.

88 r and inner mitochondrial membrane channels, voltage-dependent anion channel 1 and the mitochondrial

89 n corneal epithelia, INSR interacts with the voltage-dependent anion channel-1 (VDAC1) in mitochondri

90 ns, the most abundant OMM transporter is the voltage-dependent anion channel.

91 ) ) entry into pancreatic beta-cells through voltage-dependent Ca(2+) (Ca(V) ) channels.

92 Voltage-dependent Ca(2+) channel activity is dependent o

93 Two candidate modules featuring voltage-dependent Ca2+-channels link these outputs to th

94 The authors identify two proteins, the voltage-dependent calcium channel auxiliary subunit BARP

95 BARP, an auxiliary subunit of voltage-dependent calcium channels, promoted alpha6beta4

96 minoglycoside activity, which is ascribed to voltage-dependent drug uptake.

97 AD(P)H fluorescence signal and low uptake of voltage-dependent dyes, but are energized by a pH gradie

98 acceleration of electrochemical reactions by voltage-dependent formation of the interfacial microreac

99 esidues are important for H(+) transport and voltage-dependent gating in the CLC exchangers.

100 report a two-stage E-M coupling mechanism in voltage-dependent gating of K(V)7.1 as triggered by VSD

101 ations in nCa(V) confer unusually sensitive, voltage-dependent inactivation to inhibit responses to n

102 ntial [1], ionic gradients across cells [2], voltage-dependent ion channels [3], molecular motors [4-

103 ance, filtering of the receptor potential by voltage-dependent ion channels, is ubiquitous in all non

104 KCNQ1, also known as Kv7.1, is a voltage-dependent K(+) channel that regulates gastric ac

105 re larger in external Ba(2+) than in Ca(2+); voltage-dependent kinetics of activation, inactivation,

106 2(Q) homomeric receptors in an activity- and voltage-dependent manner, indicating a pore block mechan

107 NMDA receptor currents in a dose-, pH-, and voltage-dependent manner.

108 No voltage-dependent mechanism that synchronized Ca(2+) tra

109 -dependent CatSper dynamics articulated with voltage-dependent neutral sodium-proton exchanger (NHE).

110 p the determinants of S4 helix motion during voltage-dependent transition from the intermediate to th

111 channels, the activation of which is steeply voltage-dependent.

112 Here, we demonstrate room-temperature voltage-driven nitrogen transport (i.e., nitrogen magnet

113 entered cubic structure) and show reversible voltage-driven ON-OFF ferromagnetism.

114 lso tested by ANEPPS, FluoVolt, and ArcLight voltage dye-based APD90 measurements.

115 fferent cation configurations at the filter, voltages, electrolyte concentrations, and force-field pa

116 red CCD chloride absorption, transepithelial voltage, epithelial sodium channel activity, and pendrin

117 applications, because of their high working voltage, excellent safety, and environmental friendlines

118 ansfer is diffusion-limited, by changing the voltage excitation frequency during AC voltammetry, the

119 ient energy management of the generated high-voltage for practical low-voltage applications is still

120 chemicals by simple switching between DESI, voltage-free EASI, or LTP ionization as well as to freel

121 s to the microenvironment of the presynaptic voltage gated Ca(2+) channels revealed that alkalinizati

122 med mode of action is via blockade of axonal voltage gated potassium channels, thereby enhancing cond

123 al information processing units that rely on voltage-gated Ca(2+) (Ca(v)) channels to trigger Ca(2+)-

124 and animal models had suggested that several voltage-gated Ca(2+) channels (VGCCs) regulated critical

125 In previous studies, T-type voltage-gated Ca(2+) channels (VGCCs) were implicated in

126 To determine whether Cav1.2 voltage-gated Ca(2+) channels contribute to astrocyte ac

127 hs in our understanding of the properties of voltage-gated Ca(2+) channels that support their presyna

128 ll biology in bystander neurons, as were the voltage-gated calcium channel Cacophony (Cac) and the mi

129 ggests that BsYetJ/TMBIM6 is a pH-dependent, voltage-gated calcium channel.

130 For example, presynaptic voltage-gated calcium channels (VGCCs) and postsynaptic

131 ulation were mediated, in part, by dendritic voltage-gated calcium channels (VGCCs): pharmacological

132 n of all deletions in the significant set of voltage-gated calcium channels among CNVs called from bo

133 Deconditioning was mediated by L-type voltage-gated calcium channels and is consistent with co

134 e, we found that the alpha2delta2 subunit of voltage-gated calcium channels negatively regulates axon

135 by beta-adrenergic augmentation of Ca(V)1.2 voltage-gated calcium channels(1-4).

136 ponses in each compartment were dependent on voltage-gated calcium channels, and somatic and nuclear

137 glycosylation including glutamate receptors, voltage-gated calcium channels, the dopamine D2 receptor

138 hanisms and enter the cytosol mostly through voltage-gated calcium channels.

139 Voltage-gated calcium currents were unchanged between th

140 ential physiological relevance in control of voltage-gated calcium influx and calcium-dependent cellu

141 Gene expression of KCNA5 (potassium voltage-gated channel subfamily A member 5; encoding Kv1

142 hat Hip14 palmitoylates the Shaker-like K(+) voltage-gated channel subunit (Kv1.1), thereby regulatin

143 The evolution of Na(+)-selective four-domain voltage-gated channels (4D-Na(v)s) in animals allowed ra

144 acteria encode single-domain Na(+)-selective voltage-gated channels (BacNa(v)), they typically exhibi

145 CLC-2 is a voltage-gated chloride channel that is widely expressed

146 y and visual stimulation reveal an intrinsic voltage-gated conductance that profoundly alters the int

147 The voltage-gated Hv1 proton channel is a ubiquitous membran

148 proteins are affected as well, particularly voltage-gated ion channels (VGICs).

149 Voltage-gated ion channels endow membranes with excitabi

150 STATEMENT Changes in dendritic function, and voltage-gated ion channels in particular, are increasing

151 nalogues vary in their selectivity for human voltage-gated ion channels involved in the ventricular a

152 ry and inhibitory cell types, genes encoding voltage-gated ion channels responsible for depolarizing

153 e relationship among gating modifier toxins, voltage-gated ion channels, and the lipid membrane surro

154 tricular action potential depends on several voltage-gated ion channels, including Na(V), Ca(V), and

155 ovo missense variant in KCNA2, which encodes voltage-gated K(+) channel K(V) 1.2.

156 Voltage-gated K(+) channels function in macromolecular c

157 The function of the voltage-gated KCNQ1 potassium channel is regulated by co

158 ated by an influx of sodium (Na(+)) ions via voltage-gated Na(+) channels.

159 ha-cells is tightly linked to the opening of voltage-gated P/Q-type Ca(2+) channels, the activation o

160 Voltage-gated potassium (Kv) channels display several ty

161 The electrically silent (KvS) members of the voltage-gated potassium (Kv) subfamilies Kv5, Kv6, Kv8,

162 Voltage-gated potassium 11.1 (K(v)11.1) channels play a

163 Aminopyridine (4AP) is a specific blocker of voltage-gated potassium channels (K(V)1 family) clinical

164 Neuronal voltage-gated potassium channels (Kv) are critical regul

165 ty of the VLS, we analyzed the expression of voltage-gated potassium channels in rodent and primate b

166 Kv3 voltage-gated potassium channels mediate action potentia

167 However, in several voltage-gated potassium channels, using specific S4-S5(L

168 appeared self-inhibitory because of ClC-5's voltage-gated properties, but shunt conductance facilita

169 Voltage-gated proton channels (H(V)1) are essential for

170 )](i) changes were sensitive to the specific voltage-gated sodium (Na(V)) channel blocker tetrodotoxi

171 Voltage-gated sodium (Na(V)) channels are pore-forming t

172 a granulosa) use tetrodotoxin (TTX) to block voltage-gated sodium (Na(v)) channels as a chemical defe

173 Voltage-gated sodium (Na(V)) channels drive neuronal exc

174 ity, as the consequence of the properties of voltage-gated sodium and potassium channels.

175 Voltage-gated sodium channel (VGSC) beta1 subunits are m

176 Missense variants in the SCN8A voltage-gated sodium channel gene are linked to early-in

177 Nav1.6 is the primary voltage-gated sodium channel isoform expressed in mature

178 The voltage-gated sodium channel isoform Na(V)1.7 is highly

179 Voltage-gated sodium channel Na(v)1.5 generates cardiac

180 Voltage-gated sodium channel Na(V)1.7 is a genetically v

181 We investigated the effect of LITAF on the voltage-gated sodium channel Nav1.5, which is critical f

182 trodotoxin (TTX), a neurotoxin that binds to voltage-gated sodium channels (Na(v) proteins), arrestin

183 Voltage-gated sodium channels comprise an ion-selective

184 increase in the density of Nav1.5-generated voltage-gated sodium current I (Na) and Nav1.5 surface p

185 -related genes, as well as genes specific to voltage-gated transmembrane ion transporters.

186 of warfarin-like compounds that open the two voltage-gated type 1 potassium (K(V)1) channels K(V)1.5

187 Inwardly rectifying, voltage-gated, two-pore domain, and related K(+) channel

188 ut they are complicated to implement at such voltages higher than several hundreds of volts.

189 rstanding and mitigating degradation in high-voltage/higher-energy-density LiCoO(2)-based cells, and

190 a dramatic increase of the charge-discharge voltage hysteresis at x > 0.88.

191 d core nuclearities to control their current-voltage (I-V) characteristics in a scanning tunneling mi

192 roperties of the fabricated devices, current-voltage (I-V) measurements are carried out at 25 degrees

193 In the subsequent current-voltage (I-V) measurements to examine its breakdown beha

194 Using a short step-duration current-voltage (I-V) protocol with Xenopus oocytes expressing e

195 individual proteins at different separation voltages (i.e., different linear velocities).

196 atients, whereas EVM identified areas of low voltage in 61%.

197 vent particles; (2) applying high activation voltages in the interface of tandem-TIMS results in coll

198 ing optimal carrier density without any gate voltages, in true-equilibrium.

199 Rs and 5-HT(3AB)Rs was non-use dependent and voltage independent, suggesting bupropion is not an open

200 ate the potential of hybrid chemical-genetic voltage indicators to combine the optical performance of

201 ituted VcChiP channel was highly dynamic and voltage induced.

202 The rates of voltage-induced channel transition between the open and

203 Our data support a model of voltage-induced death, and separates aminoglycoside bact

204 The voltage-induced modulation of thromboxane receptor activ

205 fine-grained spatial pattern and the form of voltage integration determine plasticity of different ex

206 fficult challenges must be addressed if high-voltage intercalating cathodes are to be used in such ba

207 formance by mainly limiting the open circuit voltage, interfacial layers are also crucial.

208 When operated at constant trapping voltage, ions can be activated at their secular frequenc

209 The use of an alternating current (AC) voltage is a simple, versatile method of producing elect

210 The association of LA LGE with voltage is modified by ablation.

211 tably, a new concept called the minimum mean voltage is proposed as a convenient tool to evaluate the

212 , or other bilayers, where doping by applied voltage is required, rendering them essentially non-equi

213 screening cell-to-cell variations, in which voltage is the only indicator parameter independent of h

214 Memristive function at biological voltages is possible because the protein nanowires catal

215 g the time-dependence of fluctuation-induced voltages, it is found that at low temperatures the resis

216 mplementation for short-term memories at the voltage level.

217 has been proposed to explain the first-cycle voltage loss (hysteresis)(9,12-16).

218 Ts is to save the subthreshold and overdrive voltage losses.

219 ICIRD spectroscopy on the light, oxygen, or voltage (LOV) domains of the blue light receptors aureoc

220 Our results show that a low-voltage (<0.4 V) LEEFT has no obvious effect on the foll

221 Electroanatomic voltage mapping (EVM) is a promising modality for guidin

222 on was performed, in which electroanatomical voltage mapping and electroanatomical voltage mapping-gu

223 g a median of 28 min [IQR: 25 to 33 min] for voltage mapping), with a median of 16 min (IQR: 12 to 23

224 Baseline and follow-up voltage mapping, venous potentials, ostial diameters, an

225 omical voltage mapping and electroanatomical voltage mapping-guided endomyocardial biopsy showed low

226 In the last decade voltage modulation of ligand-induced GPCR activity has b

227 as a result of the emanating effective gate voltage modulations.

228 These channels open at voltages more negative than the action potential thresho

229 at ambient conditions and are driven by high voltages, no bulky pumping systems are needed, neither f

230 The single SMFC produces a voltage of 1.16 V, which is too low for practical applic

231 ted with a NiFeP nanosheets array exhibits a voltage of 1.58 V at 30 mA cm(-2) as bifunctional electr

232 ubes is improved by about 30 times at a bias voltage of 10 V.

233 (-2) at an acceleration of 1-5 G at a supply voltage of 15 V.

234 The devices produce a sustained voltage of around 0.5 volts across a 7-micrometre-thick

235 is change is well in line with the threshold voltage of the SCGT, which has been verified by correlat

236 e at 500 mA.cm(-2) with a total electrolysis voltage of ~2.2 V.

237 293 cells) cells, biochemistry, dual Ca(2+)/voltage optical mapping in intact hearts from alcohol-ex

238 pproach can also be used to improve the high-voltage performance of other batteries in a broad temper

239 During discharge, three voltage plateaus associated with three lithiation proces

240 ransitions, leading them to exhibit multiple voltage plateaus upon Na(+) extraction/insertion.

241 ambiguously confirmed by the reversal of the voltage polarity observed under two conditions: when swi

242 Here, a small voltage potential oscillation across a newly designed el

243 It is widely accepted that membrane voltage potentiates aminoglycoside activity, which is as

244 e impacts on process efficiency by increased voltage, pressure, and the pore size of filters.

245 a parameter space specifying the current and voltage profiles of six-step, ten-minute fast-charging p

246 Using standard voltage protocols, Ni(2+) -sensitive currents comprised

247 Overall, nanosecond high-voltage pulsing can be used to significantly improve the

248 In the low voltage range, a distinct drop in deadtime was observed

249 p mode (for concurrent current injection and voltage recording) or into pseudovoltage-clamp mode (for

250 during human seizures, using invasive brain voltage recordings at seizure onset.

251 redicts the phase shift in the extracellular voltage referenced to the basilar membrane at a frequenc

252 that TPC3 voltage activation depends only on voltage sensing domain 2 (VSD2) and that each of the thr

253 for signal transduction, ligand binding, and voltage sensing.

254 stitution F302L, in helix S4 of the K(V) 1.2 voltage-sensing domain (VSD).

255 The voltage-sensing domain targeting toxin BDS-I increases N

256 Voltage sensitive fluorescent dyes (VSDs) are important

257 Optical recording using voltage-sensitive fluorescent probes has provided unprec

258 Voltair consists of a voltage-sensitive fluorophore and a reference fluorophor

259 Voltage-sensitive fluorophores enable the direct visuali

260 otoinduced electron transfer triggered RhoVR voltage-sensitive indicator coupled to a chloroalkane Ha

261 eptor R295(7.40), which showed alteration of voltage sensitivity of TP receptor upon mutation.

262 Voltage sensitivity was not limited to TP receptor becau

263 Modeling studies revealed that changes in voltage sensor activation kinetics are sufficient to rep

264 esidues located at the interface between the voltage sensor and the pore domain such that the channel

265 s, due to different interactions between the voltage sensor and the pore in the different channels.

266 (OHC) nonlinear capacitance (NLC) represents voltage sensor charge movements of prestin (SLC26a5), th

267 Each subunit is composed of a voltage sensor domain (VSD), a central pore-gate domain,

268 arization is sensed by the membrane-spanning voltage sensor domain (VSD), and the cNMP-dependent gati

269 ting in large inward cation currents via the voltage sensor domain in response to PS stimulation.

270 CNQ1, at a location that appears to lock the voltage sensor in its depolarized conformation.

271 iants in a 36 base region of SCN5A in the S4 voltage sensor of domain IV and stably integrated the li

272 KAT1 displays a depolarized voltage sensor, which interacts with a closed pore domai

273 regularly spaced arginine residues in the S4 voltage sensor.

274 d receptor, and activation of an ion channel voltage-sensor domain, unraveling features critical for

275 The voltage sensors are partially activated, and the fast-in

276 A larger voltage shift of the charge neutral point was obtained d

277 derlying chemical mechanism of the threshold voltage shift to negative voltages.

278 charge offset drift measurements (measuring voltage shifts in the SET control curve).

279 hing between two isomer states by applying a voltage signal to the molecular junction, and the inform

280 ges ultranarrow pores quicker than an abrupt voltage step.

281 ork we showed for a simple model that a slow voltage sweep charges ultranarrow pores quicker than an

282 te with desired probability via a current or voltage that generates spin transfer torque, while the s

283 s (sensor charge movements out of phase with voltage) that may occur, and such loss conceivably may i

284 Specifically, above the threshold voltage, the device showed high responsivities with addi

285 rac band is slightly carrier doped by a gate voltage, the edge state starts to dissipate and exhibits

286 However, after being cycled at high voltages, these single-crystal materials exhibit severe

287 nd sodium conductance density to the somatic voltage threshold.

288 he BSI signal is sensitive to the separation voltage through the Kerr mechanism.

289 event, 1-year all-cause mortality, from ECG voltage-time traces.

290 Impedance is the ratio of voltage to current in an electrical circuit.

291 alographic (EEG) "microstates" are canonical voltage topographies that reflect brief activations of c

292 action that can be minimized by limiting the voltage used on charging.

293 We show that the piezo voltage used to maintain a null deflection provides a re

294 is a widely used medical test, consisting of voltage versus time traces collected from surface record

295 d for the retention time when the applied AC voltage was altered (increased).

296 abnormalities (right bundle branch block/low voltages) was developed to predict the presence of AS-CA

297 potentially other ion sources involving high voltage waveforms.

298 edged sword-it facilitates a large operating voltage when paired with essentially any cathode, promis

299 tuations in the plasma membrane potential or voltage, which are mediated via the activity of many ion

300 eved in a Mott insulator by applying current/voltage, which triggers an insulator-metal transition (I